Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ajm1 |
T |
C |
2: 25,469,714 (GRCm39) |
T66A |
probably benign |
Het |
Akap11 |
T |
C |
14: 78,750,869 (GRCm39) |
N506S |
probably benign |
Het |
Brinp3 |
A |
T |
1: 146,777,197 (GRCm39) |
H548L |
possibly damaging |
Het |
Cacna1c |
A |
G |
6: 118,615,407 (GRCm39) |
V1328A |
possibly damaging |
Het |
Carmil1 |
C |
T |
13: 24,339,454 (GRCm39) |
V47I |
probably damaging |
Het |
Cdk2ap2 |
C |
A |
19: 4,148,048 (GRCm39) |
T76K |
probably benign |
Het |
Col16a1 |
T |
C |
4: 129,986,564 (GRCm39) |
|
probably benign |
Het |
Cspg4b |
A |
G |
13: 113,455,703 (GRCm39) |
D583G |
probably benign |
Het |
Cxcr4 |
C |
A |
1: 128,517,362 (GRCm39) |
A100S |
probably damaging |
Het |
Fancl |
G |
T |
11: 26,419,677 (GRCm39) |
C305F |
probably damaging |
Het |
Gcnt2 |
T |
C |
13: 41,107,055 (GRCm39) |
V308A |
probably benign |
Het |
Gm11733 |
A |
T |
11: 117,375,322 (GRCm39) |
I24L |
unknown |
Het |
Gm973 |
A |
G |
1: 59,667,446 (GRCm39) |
|
probably null |
Het |
Heatr5b |
A |
T |
17: 79,109,089 (GRCm39) |
F1057I |
probably damaging |
Het |
Ifi213 |
A |
T |
1: 173,394,838 (GRCm39) |
|
probably null |
Het |
Ighv1-20 |
A |
T |
12: 114,687,471 (GRCm39) |
V91E |
probably damaging |
Het |
Inhba |
A |
G |
13: 16,201,371 (GRCm39) |
E311G |
probably damaging |
Het |
Irx3 |
G |
T |
8: 92,526,108 (GRCm39) |
|
probably null |
Het |
Jag1 |
C |
A |
2: 136,926,915 (GRCm39) |
C948F |
probably damaging |
Het |
Kcna2 |
T |
C |
3: 107,012,625 (GRCm39) |
I402T |
possibly damaging |
Het |
Kcnh8 |
A |
T |
17: 53,284,844 (GRCm39) |
Q938L |
possibly damaging |
Het |
Lrsam1 |
ACC |
AC |
2: 32,835,870 (GRCm39) |
|
probably null |
Het |
Macf1 |
T |
C |
4: 123,343,854 (GRCm39) |
T2123A |
probably benign |
Het |
Mdfic2 |
A |
T |
6: 98,215,237 (GRCm39) |
C129S |
probably damaging |
Het |
Mdh1 |
A |
T |
11: 21,509,786 (GRCm39) |
N196K |
probably benign |
Het |
Msh6 |
G |
A |
17: 88,291,989 (GRCm39) |
R248Q |
possibly damaging |
Het |
Odf2l |
G |
T |
3: 144,852,627 (GRCm39) |
R457L |
probably benign |
Het |
Or6c69c |
A |
T |
10: 129,910,898 (GRCm39) |
L206F |
probably damaging |
Het |
Pphln1 |
T |
C |
15: 93,386,856 (GRCm39) |
V318A |
possibly damaging |
Het |
Ppp1r12a |
C |
T |
10: 108,075,973 (GRCm39) |
T267I |
probably damaging |
Het |
Prpf8 |
A |
C |
11: 75,394,469 (GRCm39) |
K1801N |
possibly damaging |
Het |
Raf1 |
A |
G |
6: 115,603,667 (GRCm39) |
|
probably null |
Het |
Rasal3 |
C |
A |
17: 32,615,643 (GRCm39) |
L374F |
probably damaging |
Het |
S1pr3 |
T |
A |
13: 51,573,683 (GRCm39) |
V288D |
probably damaging |
Het |
Setd7 |
G |
A |
3: 51,428,886 (GRCm39) |
P315S |
probably benign |
Het |
Slx4 |
C |
T |
16: 3,809,404 (GRCm39) |
A364T |
probably benign |
Het |
Sp7 |
G |
A |
15: 102,267,749 (GRCm39) |
T19I |
probably benign |
Het |
Tlr9 |
T |
A |
9: 106,101,512 (GRCm39) |
C268S |
probably damaging |
Het |
Tmem117 |
T |
A |
15: 94,992,394 (GRCm39) |
D351E |
possibly damaging |
Het |
Tmem45b |
T |
A |
9: 31,339,340 (GRCm39) |
D211V |
possibly damaging |
Het |
Tns3 |
A |
G |
11: 8,401,092 (GRCm39) |
S1069P |
probably benign |
Het |
Tsnax |
A |
G |
8: 125,742,501 (GRCm39) |
I77V |
probably benign |
Het |
Txndc5 |
G |
A |
13: 38,697,101 (GRCm39) |
L79F |
possibly damaging |
Het |
Ube2q1 |
A |
G |
3: 89,684,548 (GRCm39) |
E14G |
probably benign |
Het |
Vmn2r28 |
C |
T |
7: 5,490,943 (GRCm39) |
|
probably null |
Het |
Vwde |
A |
T |
6: 13,193,117 (GRCm39) |
D407E |
probably benign |
Het |
Wdr35 |
T |
A |
12: 9,066,619 (GRCm39) |
M749K |
probably benign |
Het |
Zfp109 |
A |
T |
7: 23,928,046 (GRCm39) |
C462* |
probably null |
Het |
|
Other mutations in Pramel15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01403:Pramel15
|
APN |
4 |
144,103,703 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01516:Pramel15
|
APN |
4 |
144,104,337 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02655:Pramel15
|
APN |
4 |
144,099,416 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02983:Pramel15
|
APN |
4 |
144,099,697 (GRCm39) |
missense |
probably benign |
0.24 |
R0201:Pramel15
|
UTSW |
4 |
144,103,843 (GRCm39) |
splice site |
probably benign |
|
R1882:Pramel15
|
UTSW |
4 |
144,103,485 (GRCm39) |
missense |
probably benign |
0.03 |
R4440:Pramel15
|
UTSW |
4 |
144,099,437 (GRCm39) |
missense |
probably benign |
|
R4805:Pramel15
|
UTSW |
4 |
144,103,590 (GRCm39) |
missense |
probably benign |
0.08 |
R4823:Pramel15
|
UTSW |
4 |
144,099,781 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4925:Pramel15
|
UTSW |
4 |
144,104,502 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R5024:Pramel15
|
UTSW |
4 |
144,099,878 (GRCm39) |
nonsense |
probably null |
|
R6133:Pramel15
|
UTSW |
4 |
144,104,347 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6495:Pramel15
|
UTSW |
4 |
144,103,409 (GRCm39) |
missense |
probably benign |
0.43 |
R6585:Pramel15
|
UTSW |
4 |
144,103,600 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6732:Pramel15
|
UTSW |
4 |
144,099,743 (GRCm39) |
missense |
probably benign |
0.20 |
R7048:Pramel15
|
UTSW |
4 |
144,103,754 (GRCm39) |
missense |
probably benign |
0.15 |
R7165:Pramel15
|
UTSW |
4 |
144,099,389 (GRCm39) |
missense |
probably damaging |
0.97 |
R7469:Pramel15
|
UTSW |
4 |
144,099,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R8873:Pramel15
|
UTSW |
4 |
144,099,871 (GRCm39) |
missense |
probably benign |
0.43 |
R8891:Pramel15
|
UTSW |
4 |
144,099,397 (GRCm39) |
missense |
probably damaging |
0.99 |
R8909:Pramel15
|
UTSW |
4 |
144,103,553 (GRCm39) |
missense |
probably benign |
0.06 |
R9597:Pramel15
|
UTSW |
4 |
144,103,526 (GRCm39) |
missense |
probably damaging |
1.00 |
|